An efficient tandem approach for the synthesis of functionalized 2-pyridone-3-carboxylic acids using three-component reaction in aqueous media

Novel analogs of 2-pyridone-3-carboxylic acids 4a-l have been prepared by the three-component reaction of 3-formyl chromone, Meldrum’s acid, and primary amines in the presence of a catalytic amount of diammonium hydrogen phosphate in water. Good-to-high yields, easy work-up, and an environmentally f...

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Bibliographic Details
Main Authors: Mehrparvar, Saber (Author) , Rominger, Frank (Author)
Format: Article (Journal)
Language:English
Published: 04 May 2014
In: Molecular diversity
Year: 2014, Volume: 18, Issue: 3, Pages: 535-543
ISSN:1573-501X
DOI:10.1007/s11030-014-9522-x
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1007/s11030-014-9522-x
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Author Notes:Saber Mehrparvar, Saeed Balalaie, Mahnaz Rabbanizadeh, Elmira Ghabraie, Frank Rominger
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Summary:Novel analogs of 2-pyridone-3-carboxylic acids 4a-l have been prepared by the three-component reaction of 3-formyl chromone, Meldrum’s acid, and primary amines in the presence of a catalytic amount of diammonium hydrogen phosphate in water. Good-to-high yields, easy work-up, and an environmentally friendly profile are the advantages of this method for the synthesis of 2-pyridone-3-carboxylic acid derivatives.
Item Description:Gesehen am 24.07.2020
Physical Description:Online Resource
ISSN:1573-501X
DOI:10.1007/s11030-014-9522-x